Canonical Allele Identifier: CA508089817
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564202G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060945G>C , CM000681.2:g.49060945G>C GRCh38
NC_000019.9:g.49564202G>C , CM000681.1:g.49564202G>C GRCh37
NC_000019.8:g.54256014G>C NCBI36
NG_016289.1:g.7923C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+810C>G ENSP00000470689.1:n.243+810C>G
XM_011527575.1:c.-193C>G XP_011525877.1:n.-193C>G
XR_001753693.1:n.879+219C>G
XR_001753694.1:n.880-136C>G
Search 100 bp 5'
Search 100 bp 3'